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EnsembleCNV: an ensemble machine learning algorithm to identify and genotype copy number variation using SNP array data
The associations between diseases/traits and copy number variants (CNVs) have not been systematically investigated in genome-wide association studies (GWASs), primarily due to a lack of robust and accurate tools for CNV genotyping. Herein, we propose a novel ensemble learning framework, ensembleCNV,...
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| Publicat a: | Nucleic Acids Res |
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| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6468244/ https://ncbi.nlm.nih.gov/pubmed/30722045 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkz068 |
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